BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 11587274)

  • 1. Connexin 26 mutations: the first practical genetic marker of inherited hearing loss.
    Perry CF
    Med J Aust; 2001 Aug; 175(4):182-3. PubMed ID: 11587274
    [No Abstract]   [Full Text] [Related]  

  • 2. Connexin mutations in deafness.
    White TW; Deans MR; Kelsell DP; Paul DL
    Nature; 1998 Aug; 394(6694):630-1. PubMed ID: 9716127
    [No Abstract]   [Full Text] [Related]  

  • 3. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
    Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ
    JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness.
    Hwa HL; Ko TM; Hsu CJ; Huang CH; Chiang YL; Oong JL; Chen CC; Hsu CK
    Genet Med; 2003; 5(3):161-5. PubMed ID: 12792423
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Connexin mutations and hearing loss.
    Scott DA; Kraft ML; Stone EM; Sheffield VC; Smith RJ
    Nature; 1998 Jan; 391(6662):32. PubMed ID: 9422505
    [No Abstract]   [Full Text] [Related]  

  • 6. Gap-junction channels dysfunction in deafness and hearing loss.
    Martínez AD; Acuña R; Figueroa V; Maripillan J; Nicholson B
    Antioxid Redox Signal; 2009 Feb; 11(2):309-22. PubMed ID: 18837651
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Connexin mutation testing of children with nonsyndromic, autosomal recessive sensorineural hearing loss.
    Thomas MA; Der Kaloustian VM; Tewfik TL
    J Otolaryngol; 2004 Jun; 33(3):189-92. PubMed ID: 15841999
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene.
    Mustapha M; Salem N; Delague V; Chouery E; Ghassibeh M; Rai M; Loiselet J; Petit C; Mégarbané A
    J Med Genet; 2001 Oct; 38(10):E36. PubMed ID: 11584050
    [No Abstract]   [Full Text] [Related]  

  • 9. [From gene to disease: deafness and connexin 26].
    Hoefsloot LH; Kemperman M; Cremers CW
    Ned Tijdschr Geneeskd; 2002 Feb; 146(6):259-61. PubMed ID: 11865655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High incidence of profound deafness in an isolated community.
    Zlotogora J; Barges S
    Genet Test; 2003; 7(2):143-5. PubMed ID: 12885337
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hypogonadotrophic hypogonadism associated with prelingual deafness due to a connexin 26 gene mutation.
    Houang M; Gourmelen M; Moatti L; Le BY; Garabédian EN; Denoyelle F
    J Pediatr Endocrinol Metab; 2002 Feb; 15(2):219-23. PubMed ID: 11874189
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genetics of deafness.
    Nance WE
    Ment Retard Dev Disabil Res Rev; 2003; 9(2):109-19. PubMed ID: 12784229
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Connexin 26: required for normal auditory function.
    Kelley PM; Cohn E; Kimberling WJ
    Brain Res Brain Res Rev; 2000 Apr; 32(1):184-8. PubMed ID: 10751669
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.
    Denoyelle F; Weil D; Maw MA; Wilcox SA; Lench NJ; Allen-Powell DR; Osborn AH; Dahl HH; Middleton A; Houseman MJ; Dodé C; Marlin S; Boulila-ElGaïed A; Grati M; Ayadi H; BenArab S; Bitoun P; Lina-Granade G; Godet J; Mustapha M; Loiselet J; El-Zir E; Aubois A; Joannard A; Levilliers J; Garabédian EN; Mueller RF; Gardner RJ; Petit C
    Hum Mol Genet; 1997 Nov; 6(12):2173-7. PubMed ID: 9336442
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patients.
    Bariş I; Kilinç MO; Tolun A
    Clin Genet; 2001 Dec; 60(6):452-5. PubMed ID: 11846738
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Low prevalence of the deafness-associated 35delG mutation in the connexin-26 (GJB2) gene in a Sicilian population.
    Casale M
    Clin Genet; 2003 Jun; 63(6):541-2. PubMed ID: 12786762
    [No Abstract]   [Full Text] [Related]  

  • 17. Audiological features of GJB2 (connexin 26) deafness.
    Liu XZ; Pandya A; Angeli S; Telischi FF; Arnos KS; Nance WE; Balkany T
    Ear Hear; 2005 Jun; 26(3):361-9. PubMed ID: 15937416
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Sequence analysis of the connexin 26 genes from a deafness family with A1555G mutation in Huaiyin].
    Zhang HJ; Xu CH; Zhang YJ; Zhao SY; Geng XX; Shan YF; Fan G; Xing GQ; Shan XN; Bu XK
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2005 Sep; 40(9):678-83. PubMed ID: 16335400
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiplex detection of common mutations in the Connexin-26 gene.
    Baris I; Köksal V
    Genet Test; 2003; 7(1):63-5. PubMed ID: 12820705
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of mutations in members of the connexin gene family as a cause of nonsyndromic deafness in Taiwan.
    Yang JJ; Huang SH; Chou KH; Liao PJ; Su CC; Li SY
    Audiol Neurootol; 2007; 12(3):198-208. PubMed ID: 17259707
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.